| Title: | Example Flow Cytometry Data |
|---|---|
| Description: | A collection of raw flow cytometry data for use in vignettes for the flowPloidy package. |
| Authors: | Tyler Smith <[email protected]> |
| Maintainer: | Tyler Smith <[email protected]> |
| License: | GPL-3 |
| Version: | 1.38.0 |
| Built: | 2026-10-10 11:09:39 UTC |
| Source: | https://github.com/bioc/flowPloidyData |
A list of LMD files from analyses of the plant leaf tissue samples, co-chopped with standards with known GC (e.g., tomato, soybean etc.).
flowPloidyFiles() fpBad() fpVac()flowPloidyFiles() fpBad() fpVac()
The function flowPloidyFiles returns a vector of filenames
corresponding to the LMD files provided by this package. Individual
elements of this vector (e.g., flowPloidyFiles()[1] can be passed
to functions that load a single FCS file, such as
flowCore::read.FCS. The entire vector can be passed to
functions that load multiple files, such as
flowPloidy::histBatch.
Each element is named with the filename (without the path), so that
you can select an individual filename either by numeric index
(i.e., flowPloidyFiles()[7]) or by name
(flowPloidyFiles()["248+S.LMD"]). The names aren't meaningful to
you, of course! I added them to provide a more robust way to select an
individual file, as the order of files may change in package updates.
The individual files named in flowPloidyFiles are LMD files
generated by a Beckman-Coulter Gallios flow cytometer. They represent
a variety of samples, and some of them are low quality. They are not
ideal data sets, but rather represent a range of data quality for
assessing the performance of flowPloidy.
fpBad() and fpVac() each return the path to a single LMD
file. These are particularly poor quality files that are used in some
of the unit tests for flowPloidy. They're probably not useful
to regular users.
A named character vector of file names, including their full path in the local file system.
flowPloidyFiles() ## a character vector of file names ## Read in the first file: library(flowCore) fcs <- read.FCS(flowPloidyFiles()[1], dataset = 1, alter.names = TRUE)flowPloidyFiles() ## a character vector of file names ## Read in the first file: library(flowCore) fcs <- read.FCS(flowPloidyFiles()[1], dataset = 1, alter.names = TRUE)